EP1048738B1 - A process for the preparation of phosphatidylserines - Google Patents
A process for the preparation of phosphatidylserines Download PDFInfo
- Publication number
- EP1048738B1 EP1048738B1 EP00108605A EP00108605A EP1048738B1 EP 1048738 B1 EP1048738 B1 EP 1048738B1 EP 00108605 A EP00108605 A EP 00108605A EP 00108605 A EP00108605 A EP 00108605A EP 1048738 B1 EP1048738 B1 EP 1048738B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- phosphatides
- reaction
- serine
- phospholipase
- solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 37
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- 150000008106 phosphatidylserines Chemical class 0.000 title claims abstract description 8
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims abstract description 36
- 238000006243 chemical reaction Methods 0.000 claims abstract description 29
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 claims abstract description 27
- 102000011420 Phospholipase D Human genes 0.000 claims abstract description 22
- 108090000553 Phospholipase D Proteins 0.000 claims abstract description 22
- 239000006185 dispersion Substances 0.000 claims abstract description 18
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims abstract description 15
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 150000008104 phosphatidylethanolamines Chemical class 0.000 claims abstract description 10
- 159000000007 calcium salts Chemical class 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 38
- 239000000243 solution Substances 0.000 claims description 34
- 150000003904 phospholipids Chemical class 0.000 claims description 20
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 16
- 239000001110 calcium chloride Substances 0.000 claims description 16
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 238000001914 filtration Methods 0.000 claims description 5
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 claims description 5
- 229920000053 polysorbate 80 Polymers 0.000 claims description 5
- 238000000108 ultra-filtration Methods 0.000 claims description 5
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 claims description 4
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 238000000855 fermentation Methods 0.000 claims description 4
- 230000004151 fermentation Effects 0.000 claims description 4
- 244000005700 microbiome Species 0.000 claims description 4
- 239000007974 sodium acetate buffer Substances 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 239000012535 impurity Substances 0.000 claims description 3
- 239000000787 lecithin Substances 0.000 claims description 3
- 235000010445 lecithin Nutrition 0.000 claims description 3
- 239000012528 membrane Substances 0.000 claims description 3
- 239000011541 reaction mixture Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 claims description 2
- 238000004108 freeze drying Methods 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 239000008348 synthetic phosphatidyl choline Substances 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- HNSDLXPSAYFUHK-UHFFFAOYSA-N 1,4-bis(2-ethylhexyl) sulfosuccinate Chemical compound CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC HNSDLXPSAYFUHK-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 241000187747 Streptomyces Species 0.000 claims 1
- 235000010633 broth Nutrition 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 claims 1
- 239000012429 reaction media Substances 0.000 claims 1
- 229960001153 serine Drugs 0.000 description 20
- 102000004190 Enzymes Human genes 0.000 description 15
- 108090000790 Enzymes Proteins 0.000 description 15
- PORPENFLTBBHSG-MGBGTMOVSA-N 1,2-dihexadecanoyl-sn-glycerol-3-phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC PORPENFLTBBHSG-MGBGTMOVSA-N 0.000 description 14
- 238000004128 high performance liquid chromatography Methods 0.000 description 12
- 239000008351 acetate buffer Substances 0.000 description 9
- 239000007858 starting material Substances 0.000 description 8
- CITHEXJVPOWHKC-UUWRZZSWSA-N 1,2-di-O-myristoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC CITHEXJVPOWHKC-UUWRZZSWSA-N 0.000 description 7
- 239000008346 aqueous phase Substances 0.000 description 7
- 229960003724 dimyristoylphosphatidylcholine Drugs 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000008347 soybean phospholipid Substances 0.000 description 6
- 239000000758 substrate Substances 0.000 description 5
- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 2
- JCABVIFDXFFRMT-DIPNUNPCSA-N [(2r)-1-[ethoxy(hydroxy)phosphoryl]oxy-3-hexadecanoyloxypropan-2-yl] octadec-9-enoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OCC)OC(=O)CCCCCCCC=CCCCCCCCC JCABVIFDXFFRMT-DIPNUNPCSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 229910001424 calcium ion Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000008344 egg yolk phospholipid Substances 0.000 description 2
- 230000002255 enzymatic effect Effects 0.000 description 2
- 125000001095 phosphatidyl group Chemical group 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- ZIIUUSVHCHPIQD-UHFFFAOYSA-N 2,4,6-trimethyl-N-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=CC(C(F)(F)F)=C1 ZIIUUSVHCHPIQD-UHFFFAOYSA-N 0.000 description 1
- -1 DMPC Chemical class 0.000 description 1
- 102000015439 Phospholipases Human genes 0.000 description 1
- 108010064785 Phospholipases Proteins 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000011097 chromatography purification Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000003842 industrial chemical process Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 229940042880 natural phospholipid Drugs 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 150000008105 phosphatidylcholines Chemical class 0.000 description 1
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010512 small scale reaction Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000006439 vascular pathology Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/06—Alanine; Leucine; Isoleucine; Serine; Homoserine
Definitions
- the present invention relates to a process for the preparation of phosphatidylserines.
- the invention relates to a process for the preparation of phosphatidylserines starting from natural or synthetic phospholipids, by reacting them with serine in an aqueous medium.
- Phosphatidylserines have manifold importance, in particular in the production of pharmaceutical compositions suitable for the therapy of cerebral involutive disorders of different nature, such as senile decline or vascular pathologies, in the preparation of particular liposome formulations, and, more recently, the commercialisation of dietetic compositions containing natural lecithins, in particular soy lecithin, enriched in phosphatidyl-(L)-serine, hereinafter referred to as PS, also containing polyunsaturated fatty acid acyl residues.
- PS phosphatidyl-(L)-serine
- the process disclosed in said patent comprises the reaction of natural or synthetic phosphatides with serine in a diphasic system consisting of a solution of the starting phosphatide in an organic solvent, typically toluene, and of an aqueous solution containing Serine and phospholipase D. Keeping said system thoroughly stirred, phosphatides are transformed into PS which can be recovered from the organic phase by precipitation with acetone.
- a diphasic system consisting of a solution of the starting phosphatide in an organic solvent, typically toluene, and of an aqueous solution containing Serine and phospholipase D.
- the present invention aims at providing a process for the preparation of phosphatidylserines on an industrial scale, which overcomes the drawbacks mentioned above with reference to the prior art.
- the starting material used in the process can be either a synthetic phosphatidylcholine (PC) such as DiMyristoylPhosphatidylCholine (DMPC), or a natural phosphatidylcholine or a mixture of phospholipids such as soy or egg lecithin or one of the commercially available phospholipid mixtures obtained by partial purification of soy or egg lecithin.
- PC synthetic phosphatidylcholine
- DMPC DiMyristoylPhosphatidylCholine
- DMPC DiMyristoylPhosphatidylCholine
- the starting material should be thoroughly dispersed in an aqueous medium before the addition of the other reagents, in order to promote reactivity.
- the dispersion is carried out keeping the starting phospholipide material under stirring for 1-10 hours at 20-50°C with 3-10 volumes of water or saline solutions.
- Ionic or non-ionic surfactants can be conveniently used, more conveniently the surfactant is bis(2-ethylhexyl)sulfosuccinate sodium salt (AOT) or Tween 80 (R) in amounts from 0.01 to 0.4 g per gram of substrate.
- AOT bis(2-ethylhexyl)sulfosuccinate sodium salt
- R Tween 80
- a further feature of this invention is that it is possible to easily remove the alcohol solvents, and in particular ethanol, which often contaminate the preparations of natural phospholipids (for example phosphatidylcholine-enriched fractions obtained from soy lecithin) and which interfere in the subsequent reaction of formation of PS as they react in the presence of phospholipase D to give the corresponding phosphatidyl derivatives (such as phosphatidylethanol when ethanol is present in the mixture).
- natural phospholipids for example phosphatidylcholine-enriched fractions obtained from soy lecithin
- This removal can be conveniently carried out by dispersing the starting phospholipid in an aqueous saline solution, decanting the suspension and removing the liquid phase which contains ethanol dissolved therein.
- aqueous saline solution can be used any saline solution having sufficiently high density to easily separate the starting material, preferably a solution of calcium chloride or of sodium acetate/acetic acid buffer or of both of them.
- the starting material aqueous dispersion is added with an aqueous solution containing serine, calcium chloride, a buffer to control pH and phospholipase D.
- the amount of serine will conveniently range from 4 to 20 mols of serine per mol of phospholipid to be converted into PS.
- serine can be in the D, L or racemic forms to obtain in any case the corresponding phosphatidyl derivatives.
- Calcium chloride is the source of calcium ion which favours the phospholipase D-catalysed reactions; furthermore, the presence of calcium ion induces the separation of phosphatidylserine in an easily filterable form after completion of the reaction.
- the concentration of calcium chloride preferably ranges from 0.05 to 0.5M.
- An enzyme having a transphosphatidylating activity higher than the hydrolysing activity should conveniently be used as the enzyme for carrying out the reaction; an enzyme of fermentative origin may be advantageously used, more conveniently the enzyme obtained by fermentation of the microorganism deposited at the ATCC under the number 55717.
- the enzyme can be used either in the crude form, namely the fermentation mixture after filtering off the microorganism, or, more preferably, after purification by ultrafiltration through membrane with suitable cut-off to remove low molecular weight impurities.
- the enzyme-rich solution from the ultrafiltration can be used as it is or it can be freeze-dried to obtain the enzyme in the solid form; the enzyme amount preferably ranges from 10 to 100 units per gram of phosphatide (the enzymatic activity is determined with test described in Biotechn Techn 7 795 (1993)).
- the reaction is preferably carried out at 25 - 60°C, most preferably from 40 to 50°C.
- PS is recovered by filtration of the reaction mixture, washing the solid with water to remove Serine and the present salts.
- a particularly advantageous aspect of the process according to the invention is that the reaction product (PS) is separated from the reaction mixture in such a form that the recovery can be effected by simple filtration without need for precipitations by addition of solvents.
- the main advantage of the process according to the invention is the possibility, unexpected in view of the prior art, to carry out the transphosphatidylation reaction of phosphatidylcholine and of similar phosphatides in an aqueous medium, to obtain phosphatidylserine of good purity and in highly satisfactory yields.
- the enzymatic solution consisted of 80 ml of a phospholipase D solution of 2 U/g activity, obtained by fermentation of the microorganism deposited under the number ATCC55717, then dialysing the crude enzyme solution through an ultrafiltration membrane with cutoff 10,000 Daltons until complete removal of the low molecular weight impurities, were used as the enzyme.
- This enzyme solution was added with added 40 g of L-serine, 2.9 g of calcium chloride. The resulting solution was added to the phosphatidylcholine dispersion and the mixture was heated to 45°C.
- HPLC Composition PS 90.7%, PC 1.4%, PA (phosphatidic acid) 6.2%.
- HPLC composition PS 90.2%, PC 0.6%, PA 6.4%.
- HPLC composition PS 88.8%, PC 0.6%, PA 4.1%.
- HPLC composition PS 59.8%, PC 1.6%, PA 6.1%, PE 6.7%.
- DMPC DiMyristoylPhosphatidylcholine
- R Tween 80
- 30 ml 0.1M sodium acetate buffer pH 4.5 were stirred at 45 °C for 1 hour.
- the dispersion was added to a solution of 80 ml of aqueous phospholipase D solution obtained as described in example 1, 40 g of L-serine and 2.9 g of calcium chloride, the temperature was brought to 50°C keeping stirring for 17 hours.
- the solid was filtered, washed with water and dried. Final weight 5.4 g.
- HPLC composition PS 83.2%, PC 4.3%, PA 11.7%.
- DMPC DiMyristoylPhosphatidylcholine
- AOT 1.0 g of AOT
- 30 ml of 0.1M sodium acetate buffer pH 4.5 were stirred at 50 °C for 45 minutes.
- the dispersion was added with a solution of 80 ml of aqueous Phospholipase D solution obtained as described in example 1, 40 g of L-serine and 2.9 g of calcium chloride, the temperature was brought to 50°C keeping stirring for 20 hours. The solid was filtered, washed with water and dried. Final weight 3.66 g.
- HPLC composition PS 85.2%, PC 10.5 %, PA 3.5%.
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT1999MI000895A IT1311929B1 (it) | 1999-04-28 | 1999-04-28 | Procedimento per la preparazione di fosfatidilserine. |
| ITMI990895 | 1999-04-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1048738A1 EP1048738A1 (en) | 2000-11-02 |
| EP1048738B1 true EP1048738B1 (en) | 2003-09-17 |
Family
ID=11382830
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00108605A Expired - Lifetime EP1048738B1 (en) | 1999-04-28 | 2000-04-20 | A process for the preparation of phosphatidylserines |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6492146B1 (pt) |
| EP (1) | EP1048738B1 (pt) |
| JP (1) | JP4792154B2 (pt) |
| AT (1) | ATE250136T1 (pt) |
| DE (1) | DE60005241T2 (pt) |
| DK (1) | DK1048738T3 (pt) |
| ES (1) | ES2206099T3 (pt) |
| IT (1) | IT1311929B1 (pt) |
| PT (1) | PT1048738E (pt) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4298902B2 (ja) * | 2000-08-09 | 2009-07-22 | 株式会社ヤクルト本社 | リン脂質の製造法 |
| IT1319679B1 (it) * | 2000-12-05 | 2003-10-23 | Chemi Spa | Processo di purificazione di fosfatidilserina. |
| JP3697189B2 (ja) | 2001-01-11 | 2005-09-21 | 日清オイリオグループ株式会社 | リン脂質の塩基交換方法 |
| JP2002218991A (ja) * | 2001-01-23 | 2002-08-06 | Nof Corp | ホスファチジルセリンの製造方法 |
| US6635456B2 (en) | 2001-02-09 | 2003-10-21 | Fidia Farmaceutici S.P.A. | Procedure for the preparation of pure phosphatides with phospholipase D |
| ITPD20010031A1 (it) * | 2001-02-09 | 2002-08-09 | Fidia Farmaceutici | Procedimento per la preparazione di fosfatidi puri e loro impiego in campo cosmetico, farmaceutico ed alimentare. |
| KR20030084200A (ko) * | 2002-04-25 | 2003-11-01 | 주식회사 두산 | 비 유기용매시스템에서의 포스파티딜에탄올아민 및리소포스파티딜에탄올아민의 제조방법 및 그 방법으로제조된 리소포스파티딜에탄올아민을 포함하는 수용성 조성물 |
| KR20030086128A (ko) * | 2002-05-03 | 2003-11-07 | 주식회사 두산 | 효소 및 세린의 재사용을 포함하는 포스파티딜세린 및리소포스파티딜세린의 제조방법 |
| US6878532B1 (en) | 2003-04-28 | 2005-04-12 | Sioux Biochemical, Inc. | Method of producing phosphatidylserine |
| DE102004002053A1 (de) * | 2004-01-15 | 2005-08-04 | Bioghurt Biogarde Gmbh & Co. Kg | Verfahren zur Herstellung von Phosphatidylserin und dessen Reinigung durch Extraktion |
| JP2005318827A (ja) * | 2004-05-07 | 2005-11-17 | Nisshin Oillio Group Ltd | セリンの回収方法 |
| DE102004038443A1 (de) * | 2004-08-07 | 2006-03-16 | Bioghurt Biogarde Gmbh & Co. Kg | Verfahren zur enzymatischen Herstellung und/oder Modifikation von Phospholipiden |
| KR100598222B1 (ko) | 2004-12-16 | 2006-07-07 | 주식회사 두산 | 포스파티딜세린 및 리조포스파티딜세린의 제조방법 |
| ITPD20050164A1 (it) | 2005-05-30 | 2006-11-30 | Fidia Farmaceutici | Processo per la preparazione e l'isolamento di fosfatidi |
| RU2482186C2 (ru) | 2008-05-15 | 2013-05-20 | Лодерс Кроклан Б.В. | Способ получения фосфатидилсерина |
| RU2472351C2 (ru) | 2008-05-15 | 2013-01-20 | Лодерс Кроклан Б.В. | Способ получения фосфолипазы d |
| WO2010004597A1 (en) | 2008-07-08 | 2010-01-14 | Chemi Spa | Rocess for the production of n-acyl-phosphatidyl-etanolamine |
| US8846338B2 (en) * | 2008-08-07 | 2014-09-30 | Lipogen Ltd. | Processes for the preparation of phosphatides |
| US8546104B2 (en) * | 2008-08-07 | 2013-10-01 | Lipogen Ltd. | Processes for the preparation of phosphatide salts |
| KR101055094B1 (ko) * | 2009-05-23 | 2011-08-08 | 주식회사 고센바이오텍 | 양배추 포스포리파아제 d에 의한 난황 인지질로부터 포스파티딜세린의 생합성 방법 |
| KR101122388B1 (ko) * | 2009-05-23 | 2012-03-23 | 주식회사 고센바이오텍 | 배추 포스포리파아제 d에 의한 난황 인지질로부터 포스파티딜세린의 생합성 방법 |
| ITPD20120021A1 (it) | 2012-01-26 | 2013-07-27 | Fidia Farmaceutici | "nuove composizioni farmaceutiche contenenti fosfatidilserina e curcumina". |
| WO2016012861A1 (en) | 2014-07-25 | 2016-01-28 | Enzymotec Ltd. | Nutritional compositions containing phosphatidylserine powder |
| WO2017125816A1 (en) * | 2016-01-21 | 2017-07-27 | Enzymotec Ltd. | Methods using phosphatidylserine powder |
| CN109486790B (zh) * | 2018-12-10 | 2021-08-03 | 南通励成生物工程有限公司 | 一种以磷脂酶d转化制备磷酯酰丝氨酸的方法 |
| CN112384630B (zh) * | 2019-12-31 | 2022-04-01 | 邦泰生物工程(深圳)有限公司 | 一种磷脂酰丝氨酸酶催化生产中抗黏性的方法以及用其生产磷脂酰丝氨酸的方法 |
| WO2021134439A1 (zh) * | 2019-12-31 | 2021-07-08 | 邦泰生物工程(深圳)有限公司 | 一种提高磷脂酶d转脂活性的方法以及用其生产磷脂酰丝氨酸的方法 |
| CN114854801A (zh) * | 2022-05-18 | 2022-08-05 | 翁源广业清怡食品科技有限公司 | 一种无有机溶剂制备磷脂酰丝氨酸的方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5991898A (ja) * | 1982-11-19 | 1984-05-26 | Toyo Jozo Co Ltd | リパ−ゼ活性測定用組成物 |
| DE3671630D1 (de) * | 1985-07-03 | 1990-07-05 | Cl Pharma | Glycero-3(2)-phospho-l-serinderivate und diese enthaltende pharmazeutischen praeparate. |
| JP3791951B2 (ja) | 1995-11-08 | 2006-06-28 | 株式会社ヤクルト本社 | 多価不飽和脂肪酸含有ホスファチジルセリンを含む油脂組成物の製造方法 |
| US5700668A (en) * | 1995-12-08 | 1997-12-23 | Italfarmaco Sud S.P.A. | Process for the industrial preparation of phosphatidylserine |
| DE19917249C2 (de) * | 1999-02-26 | 2001-09-27 | Meyer Lucas Gmbh & Co | Verfahren zur Herstellung von Phosphatidylserin-Produkten |
-
1999
- 1999-04-28 IT IT1999MI000895A patent/IT1311929B1/it active
-
2000
- 2000-04-18 US US09/550,819 patent/US6492146B1/en not_active Expired - Lifetime
- 2000-04-20 PT PT00108605T patent/PT1048738E/pt unknown
- 2000-04-20 ES ES00108605T patent/ES2206099T3/es not_active Expired - Lifetime
- 2000-04-20 DK DK00108605T patent/DK1048738T3/da active
- 2000-04-20 AT AT00108605T patent/ATE250136T1/de not_active IP Right Cessation
- 2000-04-20 EP EP00108605A patent/EP1048738B1/en not_active Expired - Lifetime
- 2000-04-20 DE DE60005241T patent/DE60005241T2/de not_active Expired - Lifetime
- 2000-04-27 JP JP2000127684A patent/JP4792154B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JP2000333689A (ja) | 2000-12-05 |
| IT1311929B1 (it) | 2002-03-20 |
| DK1048738T3 (da) | 2004-01-19 |
| ES2206099T3 (es) | 2004-05-16 |
| EP1048738A1 (en) | 2000-11-02 |
| DE60005241T2 (de) | 2004-07-01 |
| DE60005241D1 (de) | 2003-10-23 |
| ATE250136T1 (de) | 2003-10-15 |
| PT1048738E (pt) | 2004-02-27 |
| US6492146B1 (en) | 2002-12-10 |
| JP4792154B2 (ja) | 2011-10-12 |
| ITMI990895A1 (it) | 2000-10-28 |
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